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Analytical Development Biotech Jobs (NOW HIRING)

Biogen

Scientist II, Analytical Development

Cambridge, MA · On-site

$117K - $157K/yr

Ph.D. with 0-3 years of relevant experience in pharmaceutical or biotech settings * M.S. with 4+ ... Proven ability to lead analytical activities for drug development programs. * Strong knowledge of ...

Biogen

Scientist II, Analytical Development

Cambridge, MA

$117K - $157K/yr

D. with 0-3 years of relevantexperiencein pharmaceuticalor biotech settings * M.S. with 4+ years of ... Proven ability to lead analytical activities for drug development programs. * Strong knowledge of ...

New

Curia, Inc.

Analytical Development Analyst II

Hopkinton, MA · On-site

$76K - $95.30K/yr

Analytical Development Analyst II in Hopkinton, MA Build your future at Curia, where our work has ... biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to ...

AMRI

Analytical Development Analyst II

Hopkinton, MA · On-site

$76K - $95.30K/yr

Analytical Development Analyst II in Hopkinton, MA Build your future at Curia, where our work has ... biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to ...

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How much do analytical development biotech jobs pay per year?

As of Jun 1, 2026, the average yearly pay for analytical development biotech in the United States is $53,418.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,500.00 and $60,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Analytical Development Biotech professional, and why are they important?

To thrive as an Analytical Development Biotech professional, you need a strong background in analytical chemistry, biochemistry, or a related field, typically supported by at least a bachelor's or master's degree. Familiarity with analytical instrumentation such as HPLC, GC, mass spectrometry, and relevant quality systems like GMP or ICH guidelines is crucial. Strong problem-solving, attention to detail, and effective communication are important soft skills for collaborating across multidisciplinary teams. These competencies ensure accurate data generation, regulatory compliance, and successful development of biotechnological products.

What are some typical challenges faced by Analytical Development professionals in the biotech industry?

Analytical Development professionals in biotech often encounter challenges such as developing robust methods for novel biologics, ensuring regulatory compliance, and adapting to rapid technological changes. They frequently work within cross-functional teams, collaborating closely with research, manufacturing, and quality assurance groups to optimize assay performance and troubleshoot issues. Staying current with evolving regulatory standards and balancing project timelines with method validation requirements are also common aspects of the role.

What is Analytical Development in biotech?

Analytical Development in biotech refers to the process of designing, developing, and validating methods to analyze biological products, such as proteins, antibodies, or cell therapies, during various stages of drug development and manufacturing. These methods are essential for ensuring the safety, quality, potency, and purity of biotechnological products. Professionals in this field work closely with research, production, and regulatory teams to ensure that analytical methods meet industry standards and comply with regulatory requirements. Analytical Development is a critical part of bringing new biopharmaceutical products from the lab to the market.

What is the difference between Analytical Development Biotech vs Quality Control Analyst?

AspectAnalytical Development BiotechQuality Control Analyst
CredentialsBachelor's/Master's in Life Sciences, Chemistry, or related fieldsBachelor's in Chemistry, Biology, or related fields; often requires GMP training
Work EnvironmentResearch labs, development departments, collaborative teamsQuality labs, manufacturing facilities, compliance-focused settings
Industry UsageDeveloping and optimizing analytical methods for biotech productsTesting and ensuring product quality and compliance with standards

Analytical Development Biotech focuses on creating and refining analytical methods during product development, while Quality Control Analysts primarily test products to ensure they meet quality standards. Both roles require similar educational backgrounds and work in laboratory settings, but their core responsibilities differ in the product lifecycle.

More about Analytical Development Biotech jobs
What cities are hiring for Analytical Development Biotech jobs? Cities with the most Analytical Development Biotech job openings:
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What job categories do people searching Analytical Development Biotech jobs look for? The top searched job categories for Analytical Development Biotech jobs are:
Analytical Development Biotech jobs near you
Infographic showing various Analytical Development Biotech job openings in the United States as of May 2026, with employment types broken down into 5% Internship, 15% Full Time, 75% Contract, and 5% Nights. Highlights an 94% Physical, and 6% Remote job distribution, with an average salary of $53,418 per year, or $25.7 per hour.
Vice President, Analytical Development

Vice President, Analytical Development

Umoja Biopharma

Louisville, CO • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 28 days ago

Job description

Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals. We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.
Umoja Biopharma - Your Body. Your Hope. Your Cure.
POSITION SUMMARY
The Vice President of Analytical Development will provide technical, operational, and strategic leadership for Umoja's analytical development organization, with responsibility for release, characterization, and lifecycle management of analytical methods supporting clinical and commercial cell and gene therapy products. Reporting to the Chief Technical Officer (CTO), this role will define and execute the company's end-to-end analytical strategy in close partnership with Quality, Manufacturing, Regulatory, and Research.
This individual will be a critical leader at the interface of Research and Discovery, GMP Manufacturing, Quality, and CMC Regulatory, with accountability for analytical method development, qualification, validation, transfer, and specification setting for GMP products. The ideal candidate brings deep regulatory experience-particularly IND and BLA submissions-strong people leadership, and a proven ability to scale analytical organizations in fast-paced biotech environments.
This position is based in Louisville, CO (preferred) or Seattle, WA.
CORE ACCOUNTABILITIES
Specific requirements include:
Strategic Leadership & Execution
  • Provide strategic leadership and operational oversight for the Analytical Development and Process Analytics teams, including routine testing to support process and product development.
  • Define and own Umoja's overarching analytical strategy across development stages, from early clinical programs through BLA and commercialization.
  • Lead the design, implementation, and continuous improvement of laboratory systems and workflows, including development of high-throughput and automated testing strategies.
  • Drive organizational change initiatives to continuously improve efficiency, quality, and business outcomes.

Analytical Development & CMC
  • Lead analytical method development, process analytics, and lifecycle management for intermediates, drug substance, and drug product testing.
  • Establish analytical strategies for specification setting, comparability, and assay robustness consistent with regulatory expectations.
  • Provide subject matter expertise to support CMC strategy, regulatory interactions, and responses to agency questions.
  • Author and be accountable for analytical sections of regulatory submissions, including INDs and BLAs.

Cross-Functional Leadership
  • Build and maintain strong cross-functional partnerships to ensure effective handoffs of technologies, methods, and data across Research, Manufacturing, Quality, and Regulatory.
  • Review CMC project plans and timelines; ensure appropriate prioritization and on-time delivery of analytical milestones.

People, Budget & External Partnerships
  • Lead strategic planning, annual goal setting, talent development, succession planning, and organizational design for the function.
  • Own OPEX and CAPEX planning and execution in collaboration with Finance and HR.
  • Ensure the organization meets budgeted financial goals and operates within approved timelines.
  • Select, manage, and oversee external contract laboratories and vendors.
  • Champion Umoja's cultural values and foster a high-performance, inclusive, and collaborative team environment.

Leadership Competencies
Setting Strategy
  • Articulates a clear, compelling vision for the Analytical Development organization aligned with Umoja's mission and long-term goals.
  • Demonstrates creativity and entrepreneurial thinking to push scientific and operational boundaries.
  • Translates strategy into realistic, executable plans with measurable outcomes.

Executing for Results
  • Sets ambitious goals and holds self and others accountable for delivery.
  • Thrives in ambiguous, rapidly evolving environments and leads effectively through change.
  • Acts with integrity, transparency, and sound judgment in decision-making.

Leading Teams
  • Builds trust, inspires collaboration, and develops talent across functions and geographies.
  • Models resilience, perseverance, and a commitment to excellence.
  • Embraces feedback, self-reflection, and continuous improvement.

Relationships & Influence
  • Builds strong, authentic relationships through emotional intelligence and clear communication.
  • Influences through credibility, passion, and purpose rather than authority alone.
  • Celebrates team success and creates a shared sense of meaning and ownership.

The successful candidate will have:
  • Advanced degree in Biology, Biochemistry, Chemistry, or a related life sciences discipline (MS or PhD preferred).
  • Minimum of 15 years of experience in biopharmaceutical development, with significant leadership experience in analytical development.
  • Minimum of 5 years' experience building, leading, and developing high-performing teams.
  • Deep expertise in analytical techniques relevant to cell and gene therapies, including flow cytometry, ELISA, qPCR, ddPCR, and cell-based assays.
  • Extensive experience authoring and supporting IND and BLA submissions and engaging with regulatory agencies.

Preferred Qualifications:
  • Strong working knowledge of analytical development, CMC regulatory strategy, and Quality systems in the cell and gene therapy space.
  • Demonstrated success scaling organizations and infrastructure in growth-stage biotech companies.
  • Strong understanding of ICH guidelines, pharmacopeial standards, and global regulations governing GMP release testing.
  • Excellent strategic, operational, financial, and business acumen.
  • Ability to manage complexity, prioritize across multiple programs, and influence across a diverse stakeholder landscape.
  • A clear vision for building a sustainable, equitable, and values-driven culture across technical functions.

Physical Requirements:
  • Ability to travel up to 20%
  • Ability to work onsite at our Louisville, CO (preferred) or Seattle, WA location

Salary Range: $310,000 - $350,000
Benefits Offerings
Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the Benefits section of our website.

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